Exploring Clinical Study Experiences of People With Post Traumatic Stress Disorder
Not yet recruiting
- Conditions
- Post Traumatic Stress Disorder
- Registration Number
- NCT06146049
- Lead Sponsor
- Power Life Sciences Inc.
- Brief Summary
Participation in post traumatic stress disorder observational study serves as a crucial contribution to advancing medical knowledge and refining the care provided to individuals facing similar health challenges.
The primary objective centers on a meticulous examination of trial completion rates and voluntary withdrawals within this distinct patient population.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 500
Inclusion Criteria
- Diagnosis of post traumatic stress disorder
- No prior treatment for post traumatic stress disorder
- Willing and able to provide informed consent.
Exclusion Criteria
- Enrolled in another research study
- Psychiatric or behavioral illness
- Inability to provide written informed consent
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rate of patients who decide to enroll in a post traumatic stress disorder clinical research. 3 months Number of post traumatic stress disorder study participants who remain in clinical study until completion. 12 months
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Power Life Sciences
🇺🇸San Francisco, California, United States